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Codis vs Bend Bioscience

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CategoryCodisBend Bioscience
Listed sitecdmocdmo
SummaryGlobal CDMO specializing in commercial-scale spray drying, amorphous solid dispersions, microencapsulation, and continuous granulation with 400,000 sq ft of GMP manufacturing across US and UK facilities.U.S. pharmaceutical CDMO offering design, development, and manufacturing from early formulation to commercial-scale production, with cGMP capabilities including spray drying, particle engineering, and complex oral dosage forms.
Services
  • Formulation Development
  • Process Development
  • CMC Analytical Development
  • Stability Testing & Storage
  • Quality Control Testing
  • CMC Regulatory Submission Support
  • Oral Solid Dosage Manufacturing
  • Secondary Packaging & Labeling
  • Formulation Development
  • Process Development
  • CMC Analytical Development
  • Stability Testing & Storage
  • Technology Transfer
  • Secondary Packaging & Labeling
  • Quality Control Testing
  • Oral Solid Dosage Manufacturing
  • Inhalation & Nasal Dosage Manufacturing
  • Topical & Semi-Solid Manufacturing
  • Sterile Fill-Finish & Aseptic Manufacturing
  • CMC Regulatory Submission Support
Modalities
  • Small Molecule
  • Small Molecule
IndicationsData not yet provided.Data not yet provided.
Locations
  • Headquarters, St. Louis, Missouri, USA
  • Microencapsulation & Continuous Granulation, St. Louis, Missouri, USA
  • Spray Drying & Commercial Manufacturing, Haverhill, England, UK
  • Manufacturing Facility, Nottingham, England, UK
  • Manufacturing Facility, Seymour, Indiana, USA
  • Bend, Bend, Oregon, United States
  • Georgia, Georgia, United States
  • Florida, Florida, United States
  • Headquarters / Manufacturing, Bend, Oregon, United States
  • Operations, Georgia, Georgia, United States
  • Operations, Florida, Florida, United States
  • Headquarters, Bend, Oregon, United States
  • Office, Georgia, Georgia, United States
  • Office, Florida, Florida, United States
Certifications
  • FDA · Identifier: 21 CFR 210/211, 110/111, 117
  • German Authorities · Identifier: Manufacturing site GMP approval (Pharmaceutical Products Act)
Data not yet provided.
ReviewsReview summary appears after site-level review signal gate opens.Review summary appears after site-level review signal gate opens.